Diagnosis, Management, & Support
Providing comprehensive care services to those with joint hypermobility & Ehlers-Danlos syndrome.
About Us
We Care.
Sueanne Baddour, DNP, APRN, FNP
Sueanne Baddour, DNP, APRN, FNP
We have a dedicated interest and passion for supporting individuals living with joint hypermobility and related heritable connective tissue disorders, such as Ehlers-Danlos syndrome (EDS). Our founder personally lives with hypermobile Ehlers-Danlos syndrome (hEDS) and understands the frustration of seeking answers and relief for symptoms
We have a dedicated interest and passion for supporting individuals living with joint hypermobility and related heritable connective tissue disorders, such as Ehlers-Danlos syndrome (EDS). Our founder personally lives with hypermobile Ehlers-Danlos syndrome (hEDS) and understands the frustration of seeking answers and relief for symptoms that are often overlooked or misunderstood. This practice was established to provide guidance, answers, and compassionate care to those who have struggled to find support.
If you suspect you may have joint hypermobility or a related genetic condition, we are here to assist you throughout your diagnostic and management journey. Our team is committed to helping you navigate the complexities of these conditions and to offering the expertise and understanding you deserve.
Sueanne Baddour, DNP, APRN, FNP
Sueanne Baddour, DNP, APRN, FNP
Sueanne Baddour, DNP, APRN, FNP
Delivering high-quality, patient-centered care is central to my practice as a nurse practitioner and healthcare provider. With over 20 years of experience in healthcare—including more than a decade in advanced practice roles—I bring a robust background in primary care, palliative care, and academia. Since 2018, I have also served as a Cli
Delivering high-quality, patient-centered care is central to my practice as a nurse practitioner and healthcare provider. With over 20 years of experience in healthcare—including more than a decade in advanced practice roles—I bring a robust background in primary care, palliative care, and academia. Since 2018, I have also served as a Clinical Assistant Professor in my local university’s graduate nursing program, further deepening my commitment to education and evidence-based practice.
Despite rapid advances in medical knowledge, it often takes years for new information to reach patients, especially those with complex conditions like hypermobility and Ehlers-Danlos syndrome (EDS). Individuals with these conditions have historically faced significant barriers within the healthcare system, including delayed or missed diagnoses and inadequate support. As someone living with hypermobile Ehlers-Danlos syndrome (hEDS) and related conditions, I have personally encountered many of these challenges. My own journey has underscored the importance of informed, compassionate care—and I recognize how much more difficult it would have been without my healthcare background.
My vision is to alleviate the frustrations faced by individuals with hEDS or other hypermobility syndromes, dysautonomia, and mast cell activation syndrome (MCAS) by providing expert care and collaborating with patients to address their comprehensive needs. I am dedicated to advancing awareness, improving access to care, and empowering patients through education and advocacy.
I have dedicated extensive time to studying hypermobility and associated conditions, including hEDS, dysautonomia, and MCAS. This comprehensive knowledge enables me to educate and raise awareness among medical professionals through presentations at medical conferences and courses. My expertise is built on a foundation of continuous learning and a commitment to sharing insights that can improve patient care and understanding of these complex conditions.
We hear you!
Sueanne Baddour, DNP, APRN, FNP
We hear you!
Awareness of hypermobile conditions, such as Ehlers-Danlos syndrome (EDS), is often lacking, leading to frustration among patients who may not receive proper evaluation or management. This lack of awareness can result in delayed diagnoses and inadequate care for individuals with these conditions.
We diagnose and treat EDS by addressing all
Awareness of hypermobile conditions, such as Ehlers-Danlos syndrome (EDS), is often lacking, leading to frustration among patients who may not receive proper evaluation or management. This lack of awareness can result in delayed diagnoses and inadequate care for individuals with these conditions.
We diagnose and treat EDS by addressing all associated symptoms and conditions, including joint hypermobility, dysautonomia (such as postural orthostatic tachycardia syndrome, POTS), mast cell activation (such as mast cell activation syndrome, MCAS), headache, fatigue, brain fog, irritable bowel syndrome (IBS), insomnia, and more. Our approach is to treat the whole-person to ensure comprehensive care.
We will listen to your symptoms, explore your diagnosis, and discuss treatment options. Our goal is to help you sort through, manage, and guide your care so that you can experience improvement in your overall functionality. We will work with you to develop a personalized treatment plan tailored to your specific needs.